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DE1300949B - Process for the preparation of derivatives of s-hexahydrotriazine - Google Patents

Process for the preparation of derivatives of s-hexahydrotriazine

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Publication number
DE1300949B
DE1300949B DEC35881A DEC0035881A DE1300949B DE 1300949 B DE1300949 B DE 1300949B DE C35881 A DEC35881 A DE C35881A DE C0035881 A DEC0035881 A DE C0035881A DE 1300949 B DE1300949 B DE 1300949B
Authority
DE
Germany
Prior art keywords
formula
hexahydrotriazine
compound
radicals
derivatives
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
DEC35881A
Other languages
German (de)
Inventor
Zingel Dieter
Dipl-Chem Dr Rolf
Zimmermann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG Werk Kalle Albert
Original Assignee
Chemische Werke Albert
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to NL129863D priority Critical patent/NL129863C/xx
Priority to DEC33424A priority patent/DE1288313B/en
Priority to DE19641544678 priority patent/DE1544678B2/en
Priority to DEC35167A priority patent/DE1232968B/en
Application filed by Chemische Werke Albert filed Critical Chemische Werke Albert
Priority to DEC35881A priority patent/DE1300949B/en
Priority to DE19651544705 priority patent/DE1544705C/en
Priority to US471745A priority patent/US3361847A/en
Priority to BE666847D priority patent/BE666847A/xx
Priority to DK362265AA priority patent/DK125715B/en
Priority to GB30109/65A priority patent/GB1056737A/en
Priority to CH813165A priority patent/CH477495A/en
Priority to NL6509253A priority patent/NL6509253A/xx
Priority to SE9455/65A priority patent/SE321573B/xx
Priority to FR24884A priority patent/FR1451422A/en
Priority to DE1670340A priority patent/DE1670340C3/en
Priority to CH669466A priority patent/CH477460A/en
Priority to AT442366A priority patent/AT262301B/en
Priority to CH676466A priority patent/CH470429A/en
Priority to SE6944/66A priority patent/SE318577B/xx
Priority to NL6606834A priority patent/NL6606834A/xx
Priority to NL6608460A priority patent/NL6608460A/xx
Priority to SE829566A priority patent/SE350973B/xx
Priority to US642271A priority patent/US3470094A/en
Priority to US678759A priority patent/US3470177A/en
Priority to DK529468A priority patent/DK133553B/en
Publication of DE1300949B publication Critical patent/DE1300949B/en
Pending legal-status Critical Current

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/42—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes polyesters; polyethers; polyacetals
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F26/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
    • C08F26/06—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F28/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/02—Halogenated hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41—Compounds containing sulfur bound to oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Fireproofing Substances (AREA)

Description

Es ist bekannt, daß sich Diene mit bestimmten ungesättigten Verbindungen nach 0. Diels und K. Alder, Liebigs Ann. Chem., 460 (1928), 98, umsetzen lassen. Gegenstand der Erfindung ist ein Verfahren zur Herstellung von Derivaten des Hexahydrotriazins der Formel in der X SO2 bzw. C = 0 bedeutet und mindestens ein, vorzugsweise mindestens zwei Reste R die Gruppe darstellt, die übrigen Reste aber auch - CH = CH2 sein können. Hal bedeutet Brom oder vorzugsweiseChlor.It is known that dienes react with certain unsaturated compounds according to 0. Diels and K. Alder, Liebigs Ann. Chem., 460 (1928), 98, can be implemented. The invention relates to a process for the preparation of derivatives of hexahydrotriazine of the formula in which X is SO2 or C = 0 and at least one, preferably at least two, radicals R is the group represents, but the remaining radicals can also be - CH = CH2. Hal means bromine or preferably chlorine.

Man erhält diese Verbindungen durch Umsetzung von s-Hexahydrotriazinderivaten der Formel in der X die angegebene Bedeutung hat, mit mindestens 1 Mol Hexahalogencyclopentadien, in dem das Halogen ein Atomgewicht von mindestens 35 und höchstens 80 hat bei einer Temperatur von 80 bis 2500 C in einem inerten Lösungsmittel. Als Hexahalogencyclopentadiene seien z. B. das Hexabromcyclopentadien und das Dibromtetrachlorcyclopentadien, vor allem aber das Hexachlorcyclopentadien genannt. Die Umsetzung mit mindestens 3 Mol Hexahalogencyclopentadien ist bevorzugt, jedoch ist auch die Anwendung eines Überschusses, z. B. 6 Mol, möglich. Auch Gemische mehrerer Hexahalogencyclopentadienderivate können verwendet werden.These compounds are obtained by reacting s-hexahydrotriazine derivatives of the formula in which X has the meaning given, with at least 1 mole of hexahalogencyclopentadiene, in which the halogen has an atomic weight of at least 35 and at most 80 at a temperature of 80 to 2500 C in an inert solvent. As Hexahalogencyclopentadien z. B. the hexabromocyclopentadiene and the dibromotetrachlorocyclopentadiene, but especially the hexachlorocyclopentadiene called. The reaction with at least 3 moles of hexahalogencyclopentadiene is preferred, but the use of an excess, e.g. B. 6 moles, possible. Mixtures of several hexahalogencyclopentadiene derivatives can also be used.

Zweckmäßig wird eine Lösung der Reaktionspartner in einem inerten organischen Lösungsmittel in Gegenwart eines Polymerisationsinhibitors, gegebenenfalls unter erhöhtem Druck erhitzt, vorzugsweise auf eine Temperatur von 90 bis 160"C. Geeignete Lösungsmittel sind z. B. Kohlenwasserstoffe, Äther, Ketone, Ester, Alkohole aliphatischer Natur, aromatische Kohlenwasserstoffe oder halogenierte aromatische oder aliphatische Kohlenwasserstoffe, wie Lackbenzin, n-Propanol, iso-Butanol, Toluol, Xylol, Mono- und Dichlorbenzol, l-Chlordekan. Die s-Hexahydrotriazinderivate scheiden sich gegen Ende der Reaktion in kristalliner Form ab oder lassen sich nach Abdestillation des Lösungsmittels durch Zusatz von z. B. A solution of the reactants in an inert one is expedient organic solvent in the presence of a polymerization inhibitor, if appropriate heated under increased pressure, preferably to a temperature of 90 to 160 "C. Suitable solvents are e.g. B. hydrocarbons, ethers, ketones, esters, alcohols aliphatic in nature, aromatic hydrocarbons or halogenated aromatic or aliphatic hydrocarbons such as mineral spirits, n-propanol, iso-butanol, toluene, Xylene, mono- and dichlorobenzene, l-chlorodecane. The s-hexahydrotriazine derivatives divide towards the end of the reaction in crystalline form or can be removed after distillation the solvent by adding z. B.

Petroläther in kristalliner Form abscheiden, je nach- dem, welches Lösungsmittel bei der Umsetzung verwendet wird. Der Polymerisationsinhibitor wird in der üblichen Menge, z. B. von 0,005 bis 0,3 0/,, bezogen auf das Gewicht der Reaktionsteilnehmer, verwendet.Separate petroleum ether in crystalline form, depending on the the which Solvent is used in the reaction. The polymerization inhibitor will in the usual amount, e.g. B. from 0.005 to 0.3 0 / ,, based on the weight of the Respondent, used.

Geeignete Verbindungen sind z. B. Hydrochinon, Mono- und Di-tert.-butyl-hydrochinon, tert.-Butylbrenzkatechin.Suitable compounds are e.g. B. hydroquinone, mono- and di-tert-butyl-hydroquinone, tert-butyl catechol.

Die erfindungsgemäß erhaltenen s-Triazinderivate sind neu. Sie können z. B. als Fungizide oder Insektizide oder als Flammschutzmittel, z. B. für Phenolharze, Epoxyharze, Thermoplasten oder cellulosehaltige Materialien Verwendung finden. The s-triazine derivatives obtained according to the invention are new. You can z. B. as fungicides or insecticides or as flame retardants, e.g. B. for phenolic resins, Find epoxy resins, thermoplastics or cellulosic materials use.

Aus der deutschen Auslegeschrift 1 182 810 ist Tri-(dibrompropionyl)-s-hexahydrotriazin als fiammwidriger Zusatz zu Thermoplasten bekannt. Die Erfahren hat jedoch gelehrt, daß sich die Verwendung dieser Verbindung in härtbaren Formmassen bei der Herstellung von Formkörpern in Eisenformen nachteilig auswirkt, indem zuweilen Verfärbungen der Formkörper auftreten. Diese Schwierigkeiten sind durch die erfindungsgemäß erhältlichen Zusätze behoben. Die Schmelzpunkte der erhaltenen Verbindungen liegen wesentlich höher als die der Vergleichsverbindung, so daß ein unerwünschtes Verdampfen oder Ausschwitzen dieser Substanzen bei Erhitzen bzw. From the German Auslegeschrift 1 182 810 is tri- (dibromopropionyl) -s-hexahydrotriazine known as a flame retardant additive to thermoplastics. However, the experienced has taught that the use of this compound in curable molding compositions in the production of moldings in iron molds has a detrimental effect by sometimes discoloration the shaped body occur. These difficulties are due to the inventively obtainable Fixed additions. The melting points of the compounds obtained are substantial higher than that of the comparison compound, so that undesirable evaporation or Exudation of these substances when heated or

Verformen von Mischungen, die diese enthalten, weit weniger auftreten kann als bei der Vergleichssubstanz.Deformation of mixtures containing these occur far less can than the reference substance.

Außerdem enthält z. B. die erfindungsgemäße Verbindung V (Beispiel 4) noch polymerisierbare Gruppen, so daß sie z. B. in ungesättigten Polyesterharzen durch Mischpolymerisation eingebaut wird. Beim Erhitzen von Formmassen aus diesen Harzen können die erfindungsgemäß erhältlichen ilammwidrigen Komponenten infolge ihrer chemischen Bindung nicht mehr herausdiffundieren oder verdampfen. Eine solche chemische Bindung kann das bekannte Bromtriazinderivat infolge seines gesättigten Charakters aber nicht eingehen. Der technische Fortschritt ist daher eindeutig gegeben. Beispiel 1 In einem 2-l-Kolben, der mit Rückflußkühler, Rührwerk, Gaseinleitungsrohr und Thermometer versehen ist, werden unter Einleiten von Kohlendioxyd 100 g 1,3,5-Tris-acryloyl-s-hexahydrotriazin (0,4 Mol) und 327,6 g Hexachlorcyclopentadien (1,2 Mol) in 800 g Xylol in Gegenwart von 0,2 g Hydrochinon unter Rühren 4 Stunden auf 130 bis 140"C erhitzt. Man erhält eine klare Lösung, die im Vakuum vom Lösungsmittel befreit wird. Der gelbliche sirupöse Rückstand wird mit 500 ml Petroläther zum Kristallisieren gebracht. Man erhält 318 g eines kristallinen farblosen Produktes vom Schmelzpunkt 315 bis 318"C, entsprechend 74,4 0/o der Theorie. Nach der Umkristallisation aus Essigester schmilzt die Verbindung bei 319 bis 320"C.In addition, z. B. the compound according to the invention V (Example 4) still polymerizable groups so that they can, for. B. is built into unsaturated polyester resins by copolymerization. When molding compositions made from these resins are heated, the flame-resistant components obtainable according to the invention can no longer diffuse out or evaporate due to their chemical bond. The known bromotriazine derivative cannot enter into such a chemical bond due to its saturated character. The technical progress is therefore clearly given. example 1 In a 2-liter flask equipped with a reflux condenser, stirrer, gas inlet tube and thermometer, 100 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine (0.4 mol) and 327.6 g of hexachlorocyclopentadiene (1.2 mol) in 800 g of xylene in the presence of 0.2 g of hydroquinone are heated for 4 hours at 130 to 140 ° C. with stirring. A clear solution is obtained which is freed from the solvent in vacuo. The yellowish syrupy residue is made to crystallize with 500 ml of petroleum ether. 318 g of a crystalline colorless product with a melting point of 315 to 318 ° C., corresponding to 74.4% of theory, are obtained. After recrystallization from ethyl acetate, the compound melts at 319 to 320.degree.

Berechnet ... C159,8301,, N 3,920/o; gefunden ... Cl 59,58 0/o, N 3,70 0Io. Calculated ... C159.8301 ,, N 3.920 / o; found ... Cl 59.58 0 / o, N 3.70 0Io.

Beispiel 2 Unter den im Beispiel 1 angegebenen Bedingungen werden 200 g 1,3, 5-Tris-acryloyl-s-hexahydrotriazin mit 655,2 g Hexachlorcyclopentadien in 1,5 1 Chlorbenzol in Gegenwart von 0,8 g Di-tert.-butylhydrochinon umgesetzt und in gleicher Weise aufgearbeitet. Example 2 Under the conditions given in Example 1 are 200 g 1,3,5-tris-acryloyl-s-hexahydrotriazine with 655.2 g hexachlorocyclopentadiene reacted in 1.5 1 of chlorobenzene in the presence of 0.8 g of di-tert-butylhydroquinone and worked up in the same way.

Man erhält 616 g, das sind 7201o der Theorie, des im Beispiel 1 angegebenen s-Hexahydrotriazinderivates.616 g, that is 720 ° of theory, of that given in Example 1 are obtained s-hexahydrotriazine derivative.

Beispiel 3 Wie im Beispiel 1 und 2 beschrieben, werden 25 g 1,3 ,5-Tris-acryloyl-s-hexahydrotriazin und 81,9 g Hexachlorcyclopentadien in 200 g 1-Chlordekan in Gegenwart von 0, 1 g tert.-Butylbrenzkatechin 11/2 Stunden auf 135 bis 1400 C erhitzt. Beim Abkühlen scheiden sich 63 g der im Beispiel 1 genannten s-Hexahydrotriazin-Verbindung ab. Schmelzpunkt 319 bis 320"C ohne Umkristallisation. Example 3 As described in Examples 1 and 2, 25 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine are used and 81.9 g of hexachlorocyclopentadiene in 200 g of 1-chlorodecane in the presence of 0.1 g Tert-butyl catechol heated to 135 to 1400 ° C. for 11/2 hours. When cooling down 63 g of the s-hexahydrotriazine compound mentioned in Example 1 separate. Melting point 319 to 320 "C without recrystallization.

Beispiel 4 250 g 1,3,5-Tris-acryloyl-s-hexahydrotriazin, 820 g Hexachlorcyclopentadien und 1 g Di-tert.-butylhydrochinon werden in 21 Xylol 4 Stunden auf 135 bis 140"C erhitzt. Aus dem Reaktionsprodukt wird das Xylol abdestilliert und der Rückstand nach Abkühlen mit 21/2 1 Petroläther versetzt. Dabei scheiden sich 999 g einer kristallinen Substanz aus (Schmelzpunkt 294° C). Diese wird abgesaugt, mit 400 mol Aceton versetzt und die Lösung auf 40"C erwärmt. Der nach dem Absaugen erhaltene Rückstand (705 g) schmilzt bei 318 bis 320"C und ist mit dem nach Beispiel 1 erhaltenen Produkt der Formel (IV) identisch. Aus der Mutterlauge erhält man nach Zugabe von 300ml Petroläther 155 g einer bei 202 bis 204° C schmelzenden Substanz der folgenden Formel Berechnet... Cl 53,58 0/o; gefunden... Cl 52,90 0/o.Example 4 250 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine, 820 g of hexachlorocyclopentadiene and 1 g of di-tert-butylhydroquinone are heated to 135 to 140 ° C. in 21 xylene for 4 hours. The xylene is made from the reaction product distilled off and, after cooling, the residue is treated with 21/2 liters of petroleum ether, 999 g of a crystalline substance separating out (melting point 294 ° C.). The residue (705 g) obtained after suctioning off melts at 318 to 320 ° C. and is identical to the product of the formula (IV) obtained according to Example 1. After adding 300 ml of petroleum ether, 155 g of one at 202 to 204 are obtained from the mother liquor ° C melting substance of the following formula Calculated ... Cl 53.58%; found ... Cl 52.90 0 / o.

Beispiel 5 25 g 1,3, 5-Tris-acryloyl-s-hexahydrotriazin, 81,9 g Hexachlorcyclopentadien und 0, 1 g Hydrochinon werden in 200 ml n-Propanol 4 Stunden unter Rückfluß (97"C) gehalten. Nach Abtrennung des Lösungsmittels im Vakuum werden dem Rückstand 200 ml Petroläther zugesetzt. Man erhält 72 g der Verbindung (IV). Example 5 25 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine, 81.9 g of hexachlorocyclopentadiene and 0.1 g of hydroquinone are refluxed in 200 ml of n-propanol for 4 hours (97 "C) held. After the solvent has been separated off in vacuo, the residue becomes 200 ml petroleum ether added. 72 g of compound (IV) are obtained.

Beispiel 6 25 g 1,3, 5-Tris-acryloyl-s-hexahydrotriazin werden mit 54,6 g Hexachlorcyclopentadien in 200 ml Xylol in Gegenwart von 0, 1 g Mono-tert.-butylhydrochinon 4 Stunden unter Rühren bei 135 bis 140"C umgesetzt. Example 6 25 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine are mixed with 54.6 g of hexachlorocyclopentadiene in 200 ml of xylene in the presence of 0.1 g of mono-tert-butylhydroquinone Reacted for 4 hours with stirring at 135 to 140 "C.

Nach Abkühlen erhält man eine klare gelbe Lösung, aus der das Lösungsmittel im Vakuum abdestilliert wird. Man erhält ein gelbes, zähflüssiges Öl als Rückstand, das mit 200 ml Petroläther versetzt und über Nacht bei Zimmertemperatur stehengelassen wird. Das Produkt erstarrt zu einer farblosen kristallisierten Substanz, die abgesaugt und mit 50 ml Petroläther gewaschen wird. Die Ausbeute beträgt 75 g (entsprechend 95,6 0/o der Theorie). Das Produkt schmilzt bei 202 bis 204"C und entspricht der Formel (I), in der zwei der Reste R die Gruppierung II bedeuten.After cooling, a clear yellow solution is obtained from which the solvent is distilled off in vacuo. A yellow, viscous oil is obtained as a residue, this is mixed with 200 ml of petroleum ether and overnight at room temperature is left standing. The product solidifies to a colorless crystallized substance, which is suctioned off and washed with 50 ml of petroleum ether. The yield is 75 g (corresponding to 95.6% of theory). The product melts at 202-204 "C and corresponds to the formula (I) in which two of the radicals R are group II.

Chlor.Chlorine.

Berechnet... 53,58 0/o; gefunden ... 52,98 0/o. Calculated ... 53.58 0 / o; found ... 52.98 0 / o.

Beispiel 7 Es werden 25 g 1,3, 5-Tris-acryloyl-s-hexahydrotriazin (0,1 Mol) mit 27, 3 g Hexachlorcyclopentadien (0,1 Mol) in 200 ml Xylol in Gegenwart von 0, 1 g Mono-tert.-butylhydrochinon in der im Beispiel 6 angegebenen Weise umgesetzt und aufgearbeitet. Example 7 25 g of 1,3,5-tris-acryloyl-s-hexahydrotriazine are obtained (0.1 mol) with 27.3 g of hexachlorocyclopentadiene (0.1 mol) in 200 ml of xylene in the presence of 0.1 g of mono-tert-butylhydroquinone in the manner indicated in Example 6 implemented and worked up.

Neben geringen Mengen nicht umgesetzten 1,3,5-Trisacryloyl-s-hexahydrotriazins besteht das Reaktionsprodukt hauptsächlichl aus einer Verbindung der Formel (1), in der nur einer der Reste R die Gruppe II darstellt. Daneben ist als Nebenprodukt noch die im Beispiel 6 genannte Verbindung enthalten.In addition to small amounts of unreacted 1,3,5-trisacryloyl-s-hexahydrotriazine the reaction product consists mainly of a compound of the formula (1), in which only one of the radicals R represents group II. Next to it is as a by-product still contain the compound mentioned in Example 6.

Das Reaktionsprodukt schmilzt bei 170 bis 185"C, nach dem Waschen in Wasser liegt der Schmelzpunkt bei 193 bis 200"C.The reaction product melts at 170 to 185 "C, after washing in water the melting point is 193 to 200 "C.

Chlor.Chlorine.

Berechnet... 40,7 0/o; gefunden... 40,1 0/o. Calculated ... 40.7 0 / o; found ... 40.1 0 / o.

Beispiel 8 4,7 g Vinylsulfonamid werden zusammen mit 1,3 g Paraformaldehyd und 0,07 g konzentrierter Schwefelsäure in ein Reaktionsgefäß eingebracht. Dieser Ansatz wird 2 Stunden lang bei einer Temperatur von 85 bis 90"C gehalten. Es entsteht ein klarer, gelber Sirup. Diese Masse wird mit 100/0aber wäßriger Natronlauge digeriert. Es entsteht eine weiße, teilweise kristalline Masse. Durch schonende Umkristallisation mit Methanol erhält man 4,4 g einer Verbindung der Formel (1) (X SO2-) vom Schmelzbereich 110 bis 130"C. Diese Verbindung neigt beim Erhitzen auf über 100"C zur Polymerisation. 4,4 g der erhaltenen Verbindung (I) werden dann mit 9,5 g Hexachlorcyclopentadien in 8 g Xylol in Gegenwart von monotertiärem Butylhydrochinon als Inhibitor umgesetzt. Example 8 4.7 g of vinyl sulfonamide are added together with 1.3 g of paraformaldehyde and 0.07 g of concentrated sulfuric acid are placed in a reaction vessel. This The batch is kept at a temperature of 85 to 90 ° C. for 2 hours. It is formed a clear, yellow syrup. This mass is digested with 100/0 but aqueous sodium hydroxide solution. A white, partially crystalline mass is created. Through gentle recrystallization with methanol, 4.4 g of a compound of the formula (1) (X SO2-) with a melting range are obtained 110 to 130 "C. This compound tends to polymerize when heated above 100" C. 4.4 g of the compound (I) obtained are then mixed with 9.5 g of hexachlorocyclopentadiene reacted in 8 g of xylene in the presence of monotertiary butylhydroquinone as an inhibitor.

Dabei wird Kohlendioxyd eingeleitet und 3 Stunden lang auf 140"C erwärmt. Man erhält 1,5 g eines schwachgelben, harzartig festen Reaktionsproduktes der Formel (11) ohne bestimmten Schmelzpunkt, worin X = -SO2- bedeutet.Carbon dioxide is passed in and the mixture is heated to 140 ° C. for 3 hours. 1.5 g of a pale yellow, resin-like solid reaction product of the formula are obtained (11) without a specific melting point, in which X = -SO2-.

Claims (5)

Patentansprüche : 1. Verfahren zur Herstellung von s-Hexahydrotriazinderivaten durch Umsetzung von s-Hexa- hydrotriazinderivaten der Formel mit konjugierten Diolefinen, d a d u r c h g ek e n n z e i c h n e t, daß die s-Hexahydrotriazinderivate gemäß Formel (1) mit mindestens 1 Mol Hexahalogencyclopentadien, in dem das Halogen ein Atomgewicht von mindestens 35 und höchstens 80 hat, bei einer Temperatur von 80 bis 250"C in einem inerten Lösungsmittel zu einer Verbindung der Formel in der X SO2 bzw. C = O bedeutet und mindestens einer der Reste R die Gruppe darstellt, in der Hal Brom oder Chlor bedeutet, die übrigen Reste R aber auch - CH = CH2 sein können, umgesetzt werden.Claims: 1. Process for the preparation of s-hexahydrotriazine derivatives by reacting s-hexahydrotriazine derivatives of the formula with conjugated diolefins, characterized in that the s-hexahydrotriazine derivatives according to formula (1) with at least 1 mole of hexahalocyclopentadiene, in which the halogen has an atomic weight of at least 35 and at most 80, at a temperature of 80 to 250 "C in an inert Solvent to a compound of the formula in which X is SO2 or C =O and at least one of the radicals R is the group represents, in which Hal is bromine or chlorine, but the remaining radicals R can also be - CH = CH2, are implemented. 2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß Verbindungen der Formel (11), in denen mindestens zwei der Reste R für den Rest III stehen, durch Umsetzung einer Verbindung der Formel (1) mit mindestens 2 Mol des Hexahalogencyclopentadiens hergestellt werden. 2. The method according to claim 1, characterized in that compounds of formula (11), in which at least two of the radicals R represent the radical III, through Reaction of a compound of the formula (1) with at least 2 mol of the hexahalogencyclopentadiene getting produced. 3. Verfahren nach Ansprüchen 1 oder 2, dadurch gekennzeichnet, daß das Halogen Chlor ist. 3. The method according to claims 1 or 2, characterized in that the halogen is chlorine. 4. Verfahren nach Ansprüchen 1 bis 3, dadurch gekennzeichnet, daß die Umsetzung bei einer Temperatur von 90 bis 160"C durchgeführt wird. 4. Process according to Claims 1 to 3, characterized in that the reaction is carried out at a temperature of 90 to 160.degree. 5. Verfahren nach Ansprüchen 1 bis 4, dadurch gekennzeichnet, daß Verbindungen der Formel (II), in denen alle drei Reste R für den Rest III stehen, in optimaler Ausbeute durch Umsetzung der Verbindung I mit 3 bis 4 Mol des Hexahalogencyclopentadiens hergestellt werden. 5. Process according to Claims 1 to 4, characterized in that Compounds of the formula (II) in which all three radicals R represent the radical III, in optimal yield by reacting the compound I with 3 to 4 mol of the hexahalogencyclopentadiene getting produced.
DEC35881A 1964-07-16 1965-05-19 Process for the preparation of derivatives of s-hexahydrotriazine Pending DE1300949B (en)

Priority Applications (25)

Application Number Priority Date Filing Date Title
NL129863D NL129863C (en) 1964-07-16
DEC33424A DE1288313B (en) 1964-07-16 1964-07-16 Triazines as flame retardant additives
DE19641544678 DE1544678B2 (en) 1964-07-16 1964-07-16 Flame-retardant additive to polyester molding compounds
DEC35167A DE1232968B (en) 1964-07-16 1965-02-24 Process for the preparation of N, N ', N "-tris- (dibromopropionyl) -hexahydrotriazine
DEC35881A DE1300949B (en) 1964-07-16 1965-05-19 Process for the preparation of derivatives of s-hexahydrotriazine
DE19651544705 DE1544705C (en) 1965-06-18 1965-06-18 Manufacture of flame-retardant molded parts from unsaturated polyester and / or polyatheracetal molding compounds
US471745A US3361847A (en) 1964-07-16 1965-07-13 Heat-curable fire-retardant moulding compositions and fire-retardants thereof
BE666847D BE666847A (en) 1964-07-16 1965-07-14
DK362265AA DK125715B (en) 1964-07-16 1965-07-15 Thermosetting, fire-resistant plastic molding compositions based on mixtures of polymerizable condensation products and monomers, containing fillers or reinforcing substances.
GB30109/65A GB1056737A (en) 1964-07-16 1965-07-15 Fire-retardants
FR24884A FR1451422A (en) 1964-07-16 1965-07-16 Preparation of non-flammable plastic moldings and flame retardant compounds
NL6509253A NL6509253A (en) 1964-07-16 1965-07-16
SE9455/65A SE321573B (en) 1964-07-16 1965-07-16
CH813165A CH477495A (en) 1964-07-16 1965-07-16 Thermosetting, flame-retardant plastic molding compounds
DE1670340A DE1670340C3 (en) 1964-07-16 1966-04-15 Process for the preparation of derivatives of hexahydro-s-triazine
CH669466A CH477460A (en) 1964-07-16 1966-05-09 Process for the preparation of derivatives of hexahydrotriazine
AT442366A AT262301B (en) 1965-05-19 1966-05-10 Process for the preparation of new hexahydrotriazine derivatives
CH676466A CH470429A (en) 1964-07-16 1966-05-10 Use of derivatives of hexahydrotriazine as polymerizable monomers
NL6606834A NL6606834A (en) 1964-07-16 1966-05-18
SE6944/66A SE318577B (en) 1964-07-16 1966-05-18
NL6608460A NL6608460A (en) 1964-07-16 1966-06-17
SE829566A SE350973B (en) 1964-07-16 1966-06-17
US642271A US3470094A (en) 1964-07-16 1967-04-10 Compositions for preparing heat-curable fire retardant molding compositions
US678759A US3470177A (en) 1964-07-16 1967-10-27 Hexahydrotriazine derivative
DK529468A DK133553B (en) 1964-07-16 1968-10-31 Halogen-containing cyclic compounds for use as flame retardants in thermosetting molding compositions.

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DEC0033423 1964-07-16
DEC33424A DE1288313B (en) 1964-07-16 1964-07-16 Triazines as flame retardant additives
DEC35167A DE1232968B (en) 1964-07-16 1965-02-24 Process for the preparation of N, N ', N "-tris- (dibromopropionyl) -hexahydrotriazine
DEC35881A DE1300949B (en) 1964-07-16 1965-05-19 Process for the preparation of derivatives of s-hexahydrotriazine
DEC0036145 1965-06-18

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DEC33424A Pending DE1288313B (en) 1964-07-16 1964-07-16 Triazines as flame retardant additives
DE19641544678 Pending DE1544678B2 (en) 1964-07-16 1964-07-16 Flame-retardant additive to polyester molding compounds
DEC35167A Pending DE1232968B (en) 1964-07-16 1965-02-24 Process for the preparation of N, N ', N "-tris- (dibromopropionyl) -hexahydrotriazine
DEC35881A Pending DE1300949B (en) 1964-07-16 1965-05-19 Process for the preparation of derivatives of s-hexahydrotriazine

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DEC33424A Pending DE1288313B (en) 1964-07-16 1964-07-16 Triazines as flame retardant additives
DE19641544678 Pending DE1544678B2 (en) 1964-07-16 1964-07-16 Flame-retardant additive to polyester molding compounds
DEC35167A Pending DE1232968B (en) 1964-07-16 1965-02-24 Process for the preparation of N, N ', N "-tris- (dibromopropionyl) -hexahydrotriazine

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BE (1) BE666847A (en)
CH (1) CH477495A (en)
DE (4) DE1288313B (en)
DK (1) DK125715B (en)
GB (1) GB1056737A (en)
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DE1288313B (en) * 1964-07-16 1969-01-30 Albert Ag Chem Werke Triazines as flame retardant additives
CH467831A (en) * 1966-01-10 1969-01-31 Ciba Geigy Curable, filler-containing, unsaturated polyester resin mixtures
US3480582A (en) * 1966-02-17 1969-11-25 American Cyanamid Co Fire-resistant fiber blends
FR2048044B1 (en) * 1969-06-30 1973-01-12 Fmc Corp
US4034136A (en) * 1969-06-30 1977-07-05 Fmc Corporation Flame-retardant resin compositions
CA927032A (en) * 1969-06-30 1973-05-22 H. Beacham Harry Flame-retardant resin compositions
FR2167293B1 (en) * 1972-01-12 1974-10-18 Ugine Kuhlmann
US3950306A (en) * 1972-06-09 1976-04-13 The Dow Chemical Company Tris-(polyhalophenoxy)-s-triazine flame retardants

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US3470177A (en) 1969-09-30
CH477495A (en) 1969-08-31
BE666847A (en) 1966-01-14
GB1056737A (en) 1967-01-25
DE1544705B2 (en) 1972-10-26
NL6509253A (en) 1966-01-17
DE1544678A1 (en) 1969-01-30
DE1288313B (en) 1969-01-30
SE321573B (en) 1970-03-09
DE1544705A1 (en) 1969-07-17
DE1232968B (en) 1967-01-26
DE1544678B2 (en) 1970-06-18
US3361847A (en) 1968-01-02
DK125715B (en) 1973-03-26

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